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Old 09-14-2006, 11:37 AM   #1
MJo
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Becky -- I am also tired for a week after Herceptin, and I also have mild nausea. The oncologist says Herceptin doesn't cause nausea (Hah!) so of course I worried that the cancer had returned. My boss who got diagnosed at the same time I did also has mild nausea after Herceptin.

Cathya -- I don't know why you are dizzy, but posssibly it's Herceptin.

Wouldn't it be nice if all the oncology doctors and nurses took a dose of every drug their patients get. Boy would they be surprised at all the side effects they now claim can't be happening. MJO
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Old 09-14-2006, 04:59 PM   #2
Hopeful
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MJo, After I read your post, I pulled out my copy of the consent form my onc had me sign before we started treatment, which stated the major side effects of Herceptin. Nausea and vomiting were on the top of the list, followed by diarrhea, which "may be severe."

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Old 09-14-2006, 06:23 PM   #3
Bev
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Hi Cathy, Anemia will also make you dizzy. I haven't heard of a correlation of herceptin and anemia, but it's an easy one to check for. BB
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Old 09-15-2006, 06:52 AM   #4
Cathya
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Hi all;

I went to the hospital for my weekly herceptin yesterday and mentioned the dizzy spells to the lovely nurse there. She told the on call doctor and we talked about it. He looked at my last cat scan and I told him my heart test was today so we agreed that we should monitor the situation for the next couple of weeks and if there was no resolution get another cat scan. He was great and I must say it was good for me that I totally understood all the possibilities which really reduces the overall stress of the situation....for both of us I'm sure. Working like a well oiled team....it's the best.

Cathy
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Cathy

Diagnosed Oct. 2004 3 cm ductal, lumpectomy Nov. 2004
Diagnosed Jan. 2005 tumor in supraclavicular node
Stage 3c, Grade 3, ER/PR+, Her2++
4 AC, 4 Taxol, Radiation, Arimidex, Actonel
Herceptin for 9 months until Muga dropped and heart enlarged
Restarting herceptin weekly after 4 months off
Stopped herceptin after four weekly treatments....score dropped to 41
Finished 6 years Arimidex
May 2015 diagnosed with ovarian cancer
Stage 1C
started 6 treatments of carboplatin/taxol
Genetic testing show BRCA1 VUS
Nice! My hair came back really curly. Hope it lasts lol. Well it didn't but I liked it so I'm now a perm lady
29 March 2018 Lung biopsy following chest CT showing tumours in pleura of left lung, waiting for results to the question bc or ovarian
April 20, 2018 BC mets confirmed, ER/PR+ now Her2-
Questions about the possibility of ovarian spread and mets to bones so will be tested and monitored for these.
To begin new drug Palbociclib (Ibrance) along with Letrozole May, 2018.
Genetic testing of ovarian tumour and this new lung met will take months.
To see geneticist to be retested for BRCA this week....still BRCA VUS
CA125 has declined from 359 to 12 as of Aug.23/18


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Old 09-16-2006, 12:35 PM   #5
MJo
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Hopeful....

When I was first diagnosed and learned about the drugs I'd be taking, I looked up all the drug information and scared myself to death about side effects. So I stopped reading about the drugs. I've been depending on the oncologist and this board for information. I think I will start reading the drug info again. I'm missing a lot of necessary info. My biggest concern is the cough, which could be due to arimidex. I can't imagine five years of this cough.
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